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Compound Detail

CHEMBL4212584

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COCC(C(=O)O[C@@H]1C/C=C/C=C/C(=O)O[C@H]([C@@H](C)[C@@H](O)[C@@H](C)CC[C@@H](OC(=O)[C@H](C)N(C)C)[C@H](C)[C@H](OC(C)=O)[C@H](C)/C=C/N(C)C=O)C/C=C/[C@H](OC)C[C@H](C)C/C=C(\C)[C@@H](OC)CC[C@@H](C)[C@@H](O)[C@@H]1C)N(C)C

Basic Information

ChEMBL ID CHEMBL4212584
Phase Preclinical
Structure Type MOL
InChI Key JMXMEKJLQWJRHY-CLBJWJGASA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

1076.5
MW (Da)

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

Natural Product First in Class Prodrug

Extended Properties

Molecular Formula C59H101N3O14
MW 1076.46

Activity Summary

IC50 1 meas. best 11.0

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
HeLa S3
CHEMBL4296436
IC50 11.0 11.0 0.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
HeLa S3 IC50 = 0.01 nM 11.0 Cytotoxicity against human HeLaS3 cells after 96 hrs by MTT assay 29042221

Literature References

PubMed DOI Target Context # Activities
29042221 10.1016/j.bmc.2017.09.044 Unchecked 2
29042221 10.1016/j.bmc.2017.09.044 HeLa S3 1

Data from ChEMBL 36 via Core Engine